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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5643255insertion1nstd207human GRCh38 chr7: 72,963,671-72,963,671 , GRCh37.p13 chr7|NW_003871064.1: 492,907-492,907 , GRCh37.p13 chr7: 72,434,202-72,434,202 TRIM74
    nsv5641083insertion1nstd207human GRCh38 chr7: 72,958,502-72,958,502 , GRCh37.p13 chr7|NW_003871064.1: 487,738-487,738 , GRCh37.p13 chr7: 72,429,033-72,429,033 TRIM74
    nsv5570217copy number variation1nstd207human GRCh38 chr7: 72,962,380-72,962,697 , GRCh37.p13 chr7: 72,432,911-72,433,228 , GRCh37.p13 chr7|NW_003871064.1: 491,616-491,933 TRIM74
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5483692copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 471,625-490,125 , GRCh38 chr7: 72,942,389-72,960,889 , GRCh37.p13 chr7: 72,412,928-72,431,420 POM121, TRIM74, 1 more genes
    nsv5481812copy number variation1nstd206human GRCh38 chr7: 72,995,890-72,995,958 , GRCh37.p13 chr7|NW_003871064.1: 525,126-525,194 , GRCh37.p13 chr7: 72,466,419-72,466,481 STAG3L3, TRIM74
    nsv5381761copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 71,847,968-73,391,310 , GRCh38.p12 chr7: 72,382,983-73,976,980 CLDN4, CLDN3, 46 more genes
    nsv5239673copy number variation1nstd204human GRCh38.p13 chr7: 72,945,201-72,963,000 , GRCh37.p13 chr7|NW_003871064.1: 474,437-492,236 , GRCh37.p13 chr7: 72,415,740-72,433,531 NSUN5P2, POM121, 1 more genes
    nsv5237280copy number variation1nstd204human GRCh38.p13 chr7: 72,974,401-72,982,100 , GRCh37.p13 chr7: 72,444,932-72,452,630 , GRCh37.p13 chr7|NW_003871064.1: 503,637-511,336 TRIM74
    nsv5237144copy number variation1nstd204human GRCh38.p13 chr7: 73,002,201-73,007,700 , GRCh37.p13 chr7: 72,472,724-72,478,223 , GRCh37.p13 chr7|NW_003871064.1: 531,437-536,936 STAG3L3, TRIM74, 1 more genes
    nsv5234786copy number variation1nstd204human GRCh38.p13 chr7: 72,944,501-72,953,600 , GRCh37.p13 chr7|NW_003871064.1: 473,737-482,836 , GRCh37.p13 chr7: 72,415,040-72,424,139 POM121, TRIM74, 1 more genes
    nsv5230830copy number variation1nstd204human GRCh38.p13 chr7: 72,969,501-72,974,100 , GRCh37.p13 chr7: 72,440,032-72,444,631 , GRCh37.p13 chr7|NW_003871064.1: 498,737-503,336 TRIM74, FKBP6P1
    nsv5230264copy number variation1nstd204human GRCh38.p13 chr7: 73,004,101-73,010,400 , GRCh37.p13 chr7|NW_003871064.1: 533,337-539,636 , GRCh37.p13 chr7: 72,474,624-72,480,921 STAG3L3, PMS2P7, 1 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4730256inversion12nstd198human GRCh38 chr7: 72,909,603-75,903,316 , GRCh37.p13 chr7|NW_003871064.1: 438,839-3,432,552 , CLDN4, 86 more genes
    nsv4729646copy number variation1nstd102humanPathogenic GRCh37 chr7: 68,977,230-73,939,510 , GRCh38.p12 chr7: 69,512,244-74,525,180 LOC105375346, ABHD11-AS1, 70 more genes
    nsv4728820copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283 FDPSP7, LOC105375352, 119 more genes
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